• Pediatr Crit Care Me · Oct 2018

    Observational Study

    Association Between Transfusion of RBCs and Subsequent Development of Delirium in Critically Ill Children.

    • Marianne E Nellis, Ruchika Goel, Sydney Feinstein, Sevini Shahbaz, Savneet Kaur, and Chani Traube.
    • Division of Pediatric Critical Care Medicine, Department of Pediatrics, Weill Cornell Medicine, New York, NY.
    • Pediatr Crit Care Me. 2018 Oct 1; 19 (10): 925-929.

    ObjectivesTo determine the temporal relationship between the transfusion of RBCs and the subsequent development of delirium in a cohort of critically ill children.DesignNested retrospective cohort study within prospective cohort study.SettingUrban academic tertiary care PICU.PatientsAll consecutive admissions from September 2014 through August 2015.InterventionsChildren were screened twice daily for delirium during their PICU admission.Measurements And Main ResultsAmong 1,547 independent admissions screened for delirium, 166 (10.7%) were transfused RBCs. Children who were transfused RBCs were more than twice as likely to be delirious during their admission compared with children who were never transfused, after controlling for known predictors of delirium development (adjusted odds ratio, 2.16; 95% CI, 1.38-3.37; p = 0.001). Among transfused children, a temporal relationship was observed between receipt of RBCs and the subsequent development of delirium. For each additional 10 mL/kg of RBCs transfused, the recipients were 90% more likely to develop delirium or coma in the 72 hours following the transfusion, after controlling for confounders (adjusted odds ratio, 1.90; 95% CI, 1.14-3.17; p = 0.01). Anemia (represented by nadir hemoglobin prior to transfusion) was not associated with delirium development.ConclusionsIn this cohort of critically ill children, there is an independent association between the receipt of an RBC transfusion and the subsequent development of delirium. Further prospective studies are warranted to replicate this finding and investigate possible pathophysiologic mechanisms for this association.

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